Label: TAG WART REMOVER liquid

  • NDC Code(s): 84023-118-01
  • Packager: Shenzhen Yangan Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 21, 2025

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Salicyic Acid......................5.0%

  • PURPOSE

    To remove warts such as plantar wart, flat wart, common wart and corns, calluses.

  • INDICATIONS & USAGE

    ·To remove warts such as plantarvart.flat wart,common wart and corns,calluses.

    ·The plantar wart is recognized by it location only on the bottom of the foot it’s tenderness,and the interruption of the footprint pattern

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • DO NOT USE

    ·On damaged skin cuts, abrasions, eczema sunburn.

    ·f you are allergic to any of the ingredients in this product.

    ·lf you are pregnant or breastfeeding

  • DOSAGE & ADMINISTRATION

    ·Wash the affected area.

    ·May soak the wart in warm water for 5 minutes.

    ·Dry area thoroughly.

    ·Using the applicator(cotton swab)apply a layer of ointment to sufficiently cover each wart

    ·Allow it to fully absorb and cover it with a bandage as needed.

    ·Repeat this procedure once or twice daily as needed (until the wart is removed)for upto12weeks.

  • WARNINGS

    ·The liquid can get easily volatilized crystallized. tighten the cap after use.

    ·Avoid long-term contact with air while using.

    ·For external use only, don’t contact with eyes or swallow. Children should use it under the supervision of adults.

  • INACTIVE INGREDIENT

    Shard paraffin, lanolin, phenol.

  • OTHER SAFETY INFORMATION

    Store between 68°F to 77°F(20°Cto25°C).

    Protect from excessive heatabove 104°F(40°C)

  • PRINCIPAL DISPLAY PANEL

    Package label

  • INGREDIENTS AND APPEARANCE
    TAG WART REMOVER 
    tag wart remover liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84023-118
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PARAFFIN (UNII: I9O0E3H2ZE)  
    LANOLIN (UNII: 7EV65EAW6H)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84023-118-0115 mL in 1 BOTTLE; Type 0: Not a Combination Product04/21/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02804/21/2025
    Labeler - Shenzhen Yangan Technology Co., Ltd. (419283765)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Yangan Technology Co., Ltd.419283765manufacture(84023-118)